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Proteomic characterization of plasma-derived clotting factor VIII-von Willebrand factor concentrates. | LitMetric

Proteomic characterization of plasma-derived clotting factor VIII-von Willebrand factor concentrates.

Electrophoresis

Proteomics Core, COBRE Center for Cancer Research Development, Rhode Island Hospital, Providence, RI, USA.

Published: October 2009

AI Article Synopsis

  • Proteomic methods identified high levels of impurities in three commercial clotting factor VIII-von Willebrand factor (FVIII/VWF) concentrates.
  • In the older concentrates, Octanate and Haemoctin, significant impurities included inter-alpha inhibitor proteins, fibrinogen, and fibronectin, along with clotting factor II, which activates FVIII.
  • The newer concentrate, Wilate, showed reduced impurities, and the use of iTRAQ labeling revealed notable batch variations, highlighting the need for detailed quality control in FVIII/VWF preparations.

Article Abstract

Proteomic methods were used to identify the levels of impurities in three commercial plasma-derived clotting factor VIII-von Willebrand factor (FVIII/VWF) concentrates. In all three concentrates, significant amounts of other plasma proteins were found. In Octanate and Haemoctin, two concentrates developed in the 1990s, the major impurities identified were inter-alpha inhibitor proteins, fibrinogen and fibronectin. These two concentrates were also found to contain additional components such as clotting factor II (prothrombin) that are known activators of FVIII. In Wilate, a recently developed FVIII/VWF concentrate, the amount of these impurities was significantly reduced. Batch-to-batch variations and differences between three investigated products were detected using iTRAQ, an isotope labeling technique for comparative MS, demonstrating the potential value of this technique for quality control analysis. The importance of thorough proteomic investigations of therapeutic FVIII/VWF preparations from human plasma is also discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030255PMC
http://dx.doi.org/10.1002/elps.200900270DOI Listing

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